37617-33-7

Basic information

• Product Name: Cyclopentanol, 2,2-dimethyl-
• Synonyms: 2,2-Dimethylcyclopentanol
• CAS NO: 37617-33-7
• Molecular Formula: C7H14 O
• Molecular Weight: 114.188
• Mol File: 37617-33-7.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 151-152 °C(Press: 744 Torr)
• Density: 0.920±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Cyclopentanol, 2,2-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclopentanol, 2,2-dimethyl-(37617-33-7)
• EPA Substance Registry System: Cyclopentanol, 2,2-dimethyl-(37617-33-7)

Safety Data

• Hazardous Substances Data: 37617-33-7(Hazardous Substances Data)

Usage

General Description

Cyclopentanol, 2,2-dimethyl- is an organic compound with the molecular formula C7H14O. It is a colorless liquid with a slight camphor-like odor. This chemical is commonly used as a solvent and as an intermediate in the production of various industrial and consumer products. It is also used in the synthesis of pharmaceuticals and agrochemicals. Additionally, Cyclopentanol, 2,2-dimethyl- is utilized in organic synthesis as a reagent in the production of other chemical compounds. Overall, this chemical plays a significant role in various industrial and commercial processes.

Upstream product

• 59383-67-4 2-cyclobutyl-propan-2-ol 
• 144-62-7 oxalic acid 
• 4541-32-6 2,2-dimethylcyclopentanone 
• 17197-84-1 5,5-dimethylcyclopent-2-enone 
• 99700-69-3 3-(3-Iodo-propyl)-2,2-dimethyl-oxirane 
• 37619-37-7 2-Methyl-2-tosyloxymethylcyclopentanon-aethylenketal 
• 16386-93-9 2,2-dimethylpent-4-enoic acid 
• 7664-93-9 sulfuric acid 
• 37619-38-8 2-methyl-2-<<<(4-methylphenyl)sulfonyl>oxy>methyl>cyclopentanone 
• 5453-88-3 ethyl 1-methyl-2-oxocyclopentane-1-carboxylate 

Downstream Products

• 17197-84-1 5,5-dimethylcyclopent-2-enone 
• 681-57-2 2,2-dimethylglutaric acid 
• 4541-32-6 2,2-dimethylcyclopentanone 
• 94844-04-9 2,2-dimethylcyclopentyl brosylate 

Relevant articles and documents

An OPAA enzyme mutant with increased catalytic efficiency on the nerve agents sarin, soman, and GP

The wild-type OPAA enzyme has relatively high levels of catalytic activity against several organophosphate G-type nerve agents. A series of mutants containing replacement amino acids at the OPAA Y212, V342, and I215 sites showed several fold enhanced catalytic efficiency on sarin, soman, and GP. One mutant, Y212F/V342L, showed enhanced stereospecificity on sarin and that enzyme along with a phosphotriesterase mutant, GWT, which had the opposite stereospecificity, were used to generate enriched preparations of each sarin enantiomer. Inhibition of acetylcholinesterase by the respective enantioenriched sarin solutions subsequently provided identification of the sarin enantiomers as separated by normal phase enantioselective liquid chromatography coupled with atmospheric pressure chemical ionization–mass spectrometry.

Asymmetric hydrogenation of tert-alkyl ketones: DMSO effect in unification of stereoisomeric ruthenium complexes

Face off: The ruthenium complexes of a new axially chiral PNNligand (L) are highly efficient in the presence of dimethylsulfoxide (DMSO) for hydrogenation of both functionalized and unfunctionalized tert-alkyl ketones. DMSO is thought to narrow down the many possible complex stereoisomers into a single facial L/Ru complex, thus enhancing the reactivity, selectivity, and productivity. Copyright

The scope and limitations of 1,3-stannyl shift-promoted intramolecular cyclizations of α-stannyl radicals with a formyl group

α-Tributylstannyl radicals can be generated from the corresponding bromides or xanthates. These radicals undergo efficient intramolecular 1,5-cyclizations with a formyl group. The resulting β-stannyl alkoxy radicals proceed through a 1,3-stannyl shift fro